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TargetGonadotropin-releasing hormone receptor
LigandBDBM50121486
Substrate/Competitorn/a
Meas. Tech.ChEBML_71600
Ki 103±n/a nM
Citation Luthin, DRHong, YTompkins, EAnderes, KLPaderes, GKraynov, EACastro, MANared-Hood, KDCastillo, RGregory, MVazir, HMay, JMAnderson, MB Characterization of mono- and diaminopyrimidine derivatives as novel, nonpeptide gonadotropin releasing hormone (GnRH) receptor antagonists. Bioorg Med Chem Lett12:3635-9 (2002) [PubMed]
More Info.:Get all data from this article,  Assay Method
 
Gonadotropin-releasing hormone receptor
Name:Gonadotropin-releasing hormone receptor
Synonyms:GNRHR | GNRHR_HUMAN | GRHR | GnRH receptor | GnRH-R | Gonadotropin releasing hormone 1 (GnRHR1) | Gonadotropin-releasing hormone receptor | Gonadotropin-releasing hormone receptor (GnRH)
Type:Enzyme
Mol. Mass.:37749.45
Organism:Homo sapiens (Human)
Description:P30968
Residue:328
Sequence:
MANSASPEQNQNHCSAINNSIPLMQGNLPTLTLSGKIRVTVTFFLFLLSATFNASFLLKL
QKWTQKKEKGKKLSRMKLLLKHLTLANLLETLIVMPLDGMWNITVQWYAGELLCKVLSYL
KLFSMYAPAFMMVVISLDRSLAITRPLALKSNSKVGQSMVGLAWILSSVFAGPQLYIFRM
IHLADSSGQTKVFSQCVTHCSFSQWWHQAFYNFFTFSCLFIIPLFIMLICNAKIIFTLTR
VLHQDPHELQLNQSKNNIPRARLKTLKMTVAFATSFTVCWTPYYVLGIWYWFDPEMLNRL
SDPVNHFFFLFAFLNPCFDPLIYGYFSL
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  Blast E-value cutoff:
BDBM50121486
n/a
NameBDBM50121486
Synonyms:5-(3,5,5,8,8-Pentamethyl-5,6,7,8-tetrahydro-naphthalen-2-ylmethyl)-furan-2-carboxylic acid {4-[(2-chloro-pyrimidin-4-ylamino)-methyl]-cyclohexylmethyl}-amide | CHEMBL121576
TypeSmall organic molecule
Emp. Form.C33H43ClN4O2
Mol. Mass.563.173
SMILESCc1cc2c(cc1Cc1ccc(o1)C(=O)NCC1CCC(CNc3ccnc(Cl)n3)CC1)C(C)(C)CCC2(C)C |(-2.48,-15.18,;-3.84,-14.47,;-5.21,-15.18,;-6.57,-14.47,;-6.57,-13.03,;-5.21,-12.32,;-3.84,-13.03,;-2.49,-12.3,;-1.12,-13.02,;-1.12,-14.46,;1.6,-14.47,;1.6,-13.03,;.24,-12.3,;2.97,-12.32,;2.97,-10.87,;4.33,-13.03,;5.82,-12.14,;7.32,-12.98,;7.35,-14.71,;8.84,-15.55,;10.33,-14.67,;11.84,-15.52,;13.34,-14.63,;14.84,-15.47,;16.33,-14.58,;17.83,-15.42,;17.85,-17.16,;16.36,-18.06,;16.39,-19.78,;14.86,-17.2,;10.31,-12.95,;8.8,-12.09,;-7.91,-12.32,;-6.57,-11.59,;-9.29,-11.59,;-9.27,-13.03,;-9.27,-14.47,;-7.91,-15.18,;-9.29,-15.89,;-6.57,-15.91,)|
Structure
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